A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2570n100



Internal ID19012938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34447659..34585552hg38UCSC Ensembl
chr15:34739860..34877753hg19UCSC Ensembl
chr15:32527152..32665045hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38137894
hg19137894
hg18137894
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046403, nsv1043143, nsv1054558, nsv1044129, nsv1048967, nsv1037513, nsv1042030, nsv1047201, nsv1050556, nsv1054857
Samples
Known GenesGOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2570n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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